FDA Pharmaceutical Quality Training Modules
These comprehensive training modules bridge regulatory science with practical implementation.
The content provides essential expertise in pharmaceutical quality regulation, supply chain integrity, and manufacturing innovation – equipping professionals with the knowledge to navigate today's complex regulatory landscape and ensure patient safety worldwide.
Browse courses available on demand:
| Summary | Course Description |
|---|---|
| Pharmaceutical Quality Symposium 2023: Quality, Supply Chain & Advanced Manufacturing | Discover a comprehensive learning framework that progresses from foundational quality assessment principles through advanced manufacturing technologies, demonstrating how regulatory science evolves to address emerging challenges in pharmaceutical development. |
| Generic Drugs Forum (GDF) 2025 | Individual sessions provided by subject matter experts from FDA | CDER Office of Pharmaceutical Quality (OPQ) as related to generic drugs |
| Generic Drugs Forum (GDF) 2024: Regulatory Considerations to Enhance Generic Drug Access | |
| Generic Drugs Forum (GDF) 2023: Celebrating 10 Years of the GDF |
More about FDA's Center for Drug Evaluation and Research's (CDER) Small Business and Industry Assistance (SBIA) Program
CDER SBIA serves as the primary point of contact for pharmaceutical industry seeking to connect with the Agency. Our mission is to help you navigate FDA's extensive regulatory landscape and master human drug product regulation requirements. Learn more here or watch our video below. Find additional resources for professional development in the CDER SBIA Learn Online Training Repository.